Canonical Allele Identifier: CA357247228

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286001G>T (hg19) ; chr4:g.73420284G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420284G>T , CM000666.2:g.73420284G>T	GRCh38
NC_000004.11:g.74286001G>T , CM000666.1:g.74286001G>T	GRCh37
NC_000004.10:g.74504865G>T	NCBI36
NG_009291.1:g.21030G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1816G>T MANE Select	ENSP00000295897.4:p.Ala606Ser
ENST00000295897.8:c.1816G>T	ENSP00000295897.4:p.Ala606Ser
ENST00000401494.7:c.1471G>T	ENSP00000384695.3:p.Ala491Ser
ENST00000415165.6:c.1240G>T	ENSP00000401820.2:p.Ala414Ser
ENST00000476441.6:c.*1095G>T	ENSP00000423727.1:n.*1095G>T
ENST00000495173.1:n.124G>T
ENST00000503124.5:c.1366G>T	ENSP00000421027.1:p.Ala456Ser
ENST00000505649.5:n.1363G>T
ENST00000508932.5:n.206G>T
ENST00000509063.5:c.1785+645G>T	ENSP00000422784.1:n.1785+645G>T
ENST00000511370.1:c.1349G>T
ENST00000621085.4:c.1177G>T	ENSP00000483421.1:p.Ala393Ser
ENST00000621628.4:c.1177G>T	ENSP00000480485.1:p.Ala393Ser
NM_000477.5:c.1816G>T	NP_000468.1:p.Ala606Ser
NM_000477.6:c.1816G>T	NP_000468.1:p.Ala606Ser
NM_000477.7:c.1816G>T MANE Select	NP_000468.1:p.Ala606Ser